GCP compliance and readability of informed consent forms from an emerging hub for clinical trials

Background: The rapid expansion of trials in emerging regions has raised valid concerns about research subject protection, particularly related to informed consent. The purpose of this study is to assess informed consent form (ICF) compliance with Good Clinical Practice (GCP) guidelines and the read...

Full description

Bibliographic Details
Main Authors: Satish Chandrasekhar Nair, Halah Ibrahim
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2015-01-01
Series:Perspectives in Clinical Research
Subjects:
Online Access:http://www.picronline.org/article.asp?issn=2229-3485;year=2015;volume=6;issue=2;spage=104;epage=108;aulast=Nair